Busqueda de Subestructura

CC1CCC(N1)C

OC[C@H]1CC[C@@H](c2cc(F)c(F)c(F)c2)N1
Reaction #44614
title compound
Rendimiento 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #56014
benzyl 3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
Rendimiento 94.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CC2CCC(C1)N2Cc1ccc2ccccc2c1
Reaction #58205
pasty oil
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1CC2CCC(C1)N2Cc1ccc2ccccc2c1
Reaction #58206
oily product
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NC(=O)C1CC2CCCCC2N1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(O)C(=O)OCC
Reaction #70196
32
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C2CCC1CC(n1cc(-c3ccc(Oc4ccccc4)cc3)c3c(N)ncnc31)C2
Reaction #79788
3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]-8-methyl-8-azabicyclo[3.2.1]octane
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)C1=C(C(=O)OCc2ccccc2)N2C(=O)CC2C1
Reaction #96210
benzyl 3-ethylsulphinyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
Rendimiento 94.7%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(N2C3CCC2COC3)nc(Cl)n1
Reaction #162612
title compound
Rendimiento 75.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-c2nc(N3C4CCC3COC4)cc(N3C4CCC3COC4)n2)cc1
Reaction #162614
title compound
Rendimiento 45.9%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-c2nc(Cl)cc(N3C4CCC3COC4)n2)cc1
Reaction #162629
title compound
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1nc(N2C3CCC2COC3)c(Cl)c(N2C3CCC2COC3)n1
Reaction #162634
title compound
DOI: 10.6084/m9.figshare.5104873.v1
ClCc1cc(N2C3CCC2COC3)nc(Cl)n1
Reaction #162639
8-(2-chloro-6-(chloromethyl)pyrimidin-4-yl)-3-oxa-8-azabicyclo[3.2.1]octane
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(c2ccc(OC)c(C)c2C)N1
Reaction #176912
DOI: 10.1039/C8SC04228D
C#CC1CCC(C(N)=O)N1C(=O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #183786
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(C(=O)OC(C)(C)C)C(C(=O)N2C3CCC2COC3)C1
Reaction #187327
DOI: 10.1039/C8SC04228D
Nc1nc(CC(=O)Nc2ccc(CC3CCC(C(O)c4ccccc4)N3)cc2Br)cs1
Reaction #187494
DOI: 10.1039/C8SC04228D
Clc1nc(N2CCOCC2)nc(N2C3CCC2COC3)n1
Reaction #188878
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(CCc2ccccc2C(=O)N2CCNCC2)NC(CC(=O)N2CCN(C3CC4CCC(C3)N4C)CC2)=C(C(=O)OC)C1c1c(Cl)cccc1Cl
Reaction #197631
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(C(=O)OC(C)(C)C)N(C(=O)CNC(=O)OC(C)(C)C)C1c1ccccc1
Reaction #202381
DOI: 10.1039/C8SC04228D
O=C(C1CC2(c3ccccc3)NC1CCC2OCc1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCN(Cc2ccccc2)CC1
Reaction #205185
DOI: 10.1039/C8SC04228D
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